Temporary - Clinical Research Coordinator

(ID: 2026-2380) Axle is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations nationally and abroad. With experts in biomedical science, software engineering, and program management, we focus on developing and applying research tools and techniques to empower decision-making and accelerate research discoveries. We work with some of the top research organizations and facilities in the country including multiple institutes at the National Institutes of Health (NIH).

Axle is seeking a Clinical Research Coordinator (Temporary – Approximately 4 Months) to join our vibrant team at the National Institutes of Health (NIH) in Baltimore, MD. This position will support ongoing clinical research activities within the National Institute on Drug Abuse (NIDA) and offers an opportunity to contribute to cutting-edge behavioral and clinical research initiatives.

Benefits

We Offer: 100% Medical, Dental & Vision Coverage for Employees Paid Time Off and Paid Holidays 401K match up to 5% Educational

for Career Growth Employee Referral Bonus Flexible Spending Accounts: Healthcare (FSA) Parking Reimbursement Account (PRK) Dependent Care Assistant Program (DCAP) Transportation Reimbursement Account (TRN) Position Information: Under this task order, the contractor will independently provide support services to satisfy the overall operational objectives of the National Institute on Drug Abuse. The primary objective is to provide services and deliverables through performance of support services.

Qualifications

Certifications & Licenses: Minimum of one (1) year of experience in behavioral counseling, preferably in drug/smoking/alcohol treatment. Minimum of three (3) years of experience in a research related field. Master’s degree in psychology, social work, biological sciences or related discipline.

Basic Life Support (BLS) certification will be required – training will be provided. g. Microsoft Office) Skills: Will complete all NIH/NIDA Mandatory trainings or/and other required trainings by the deadline set forth.

Excellent analytical, organizational and time management skills required. Strong communications skills, both oral and written. Exceptional interpersonal skills, customer service oriented and client focused approach to work due to extensive participant contact.

Previous experience in human subjects’ interaction (clinical or research). Previous clinical trial work Deliverables: Work products and documents related to administering mental health assessments and diagnostic interviews. - Ad-Hoc Work products and documents related to obtaining participant medical and drug use information according to protocol criteria.

- Ad-Hoc Work products and documents related to obtaining informed consent documentation from participants in the screening protocol. - Ad-Hoc Work products and documents related to follow-up correspondence to candidates on recruiting status. - Ad-Hoc Work products and documents related to arranging travel and distributing remuneration for candidates.

- Ad-Hoc Work products and documents related to scheduling phone screen scripts, in person screening appointments and communications with candidates. , generating reports; perform study procedures; process and destroy specimens as needed; maintain storage records/inventory of biological specimens. - Ad-Hoc Statement of Work Details: Assist preparing and submitting for review accurate source documents related to all research procedures .

- 1 Participate in developing and maintaining research protocol documentation and operations.